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Adrenocortical tumors are rare in children and present with variable signs depending on the type of hormone excess. We herein describe the unusual presentation of a child with adrenocortical tumor and introduce the concept of in vitro chemosensitivity ...
Mullis, Primus E +5 more
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Estrogen-secreting adrenocortical tumor in a postmenopausal woman: a challenging diagnosis. [PDF]
Mermejo LM +8 more
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Successful transcatheter arterial embolization for ruptured adrenocortical tumor in a pediatric patient. [PDF]
Yoshida M +4 more
europepmc +1 more source
Combination of sorafenib and everolimus impacts therapeutically on adrenocortical tumor models.
Treatment options are insufficient in patients with adrenocortical carcinoma. Based on efficacy of sorafenib, a tyrosine kinase inhibitor, and everolimus, an inhibitor of the mammalian target of rapamycin (mTOR) in tumors of different histotype, we aimed
Cicala MV +10 more
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Oncocytic adrenocortical tumor with uncertain malignant potential in pediatric population: A case report and review of literature. [PDF]
Chen XC, Tang YM, Mao Y, Qin DR.
europepmc +1 more source
A case of infantile virilizing adrenocortical tumor [PDF]
The patient was a 16-month-old girl, born by mature natural delivery and weighing 3, 320 g. Hirsutism was noted on birth. Development of pubic hair and hypertrophy of the labia minora were noted after 8 months. At the time of admission, the height was 80
平尾, 佳彦 +10 more
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In the setting of metastatic adrenocortical cancer, there are limited therapy options such as mitotane and platinum-based chemotherapy with only low response rates. Ipilimumab and nivolumab are approved for several solid cancer types.
Rebekka Mispelbaum +5 more
doaj +1 more source
Etoposide Triggers Cellular Senescence by Inducing Multiple Centrosomes and Primary Cilia in Adrenocortical Tumor Cells. [PDF]
Teng YN +5 more
europepmc +1 more source
Carcinoma adreno-cortical: análise de 29 casos [PDF]
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina. Curso de Medicina.
Silva, Ricardo Kupka da
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SUMMARY The occurrence of metachronous adrenocortical carcinoma has rarely been described. We report a case of a child with virilizing adrenocortical metachronous tumors that, despite several metastases, presented long-term survival (15 years).
Oliveira Lima +11 more
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